Who have Oral leukoedema with Maxzide - from FDA reports

There is no Oral leukoedema reported by people who take Maxzide yet. This review analyzes which people have Oral leukoedema with Maxzide. It is created by eHealthMe based on reports from FDA, and is updated regularly.

How to use this study: bring a copy to your health teams to ensure drug risks and benefits are fully discussed and understood.

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On Feb, 11, 2019

No report is found.

Do you have Oral leukoedema while taking Maxzide?

You are not alone:

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Maxzide has active ingredients of hydrochlorothiazide; triamterene. It is often used in high blood pressure. (latest outcomes from Maxzide 8,099 users)

Oral Leukoedema

Oral leukoedema (a greyish-white lesion of the oral mucosa) has been reported by people with gastroesophageal reflux disease, osteoporosis, hypothyroidism, hypersensitivity, heart rate irregular (latest reports from 5 Oral leukoedema patients).

Drugs that are associated with Oral leukoedema
Oral leukoedema
Could your condition cause Oral leukoedema
Oral leukoedema
Maxzide side effects

Browse by gender and age

Female: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+

Male: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+

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Compare Maxzide to similar drugs:

What would happen?

Predict new side effects and undetected conditions when you take Maxzide and have Oral leukoedema

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NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.

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DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only, and has not been supported by scientific studies or clinical trials unless otherwise stated. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.

You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).

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